A Perplexing Case of a Germ Cell Tumor: A Case Report

Author:

Rajan Priyank1,Misra Ruchira1,Mushrif Sujata1,Kandalkar Bhuvaneswari2,Parikh Ruchi3,Shah Rasiklal4,Kurkure Purna1

Affiliation:

1. Department of Paediatric Hematology Oncology

2. Department of Paediatric Pathology

3. Department of Paediatric Endocrinology

4. Department of Paediatric Surgery, SRCC Children’s Hospital, Managed by Narayana Health, Mumbai, MH, India

Abstract

Germ cell tumors (GCTs) are associated with pure gonadal dysgenesis or Swyer syndrome. Swyer syndrome usually presents with primary amenorrhea, streak ovaries, and mixed GCT. However, our patient presented with secondary amenorrhea, normal female external genitalia, and a mixed GCT. Constitutional karyotype was suggestive of 46,XY. Management comprised chemotherapy, followed by surgery. Histopathology was suggestive of dysgerminoma complicating a gonadoblastoma. The purpose of reporting this case is its rarity and the importance of diagnosing an XY karyotype, as the incidence of GCTs is higher in these patients.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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